5-HIAA(5-Hydroxyindoleacetic Acid) ELISA Kit
SKU: E-EL-0075
5-HIAA(5-Hydroxyindoleacetic Acid) ELISA Kit
Detection Range | 1.56-100 ng/mL |
Sensitivity | 0.94 ng/mL |
Product Details
Properties
Assay Type | Competitive-ELISA |
size | 96T |
Assay Time | 2.5h |
Detection Method | Colormetric |
Detection Range | 1.56-100 ng/mL |
Sensitivity | 0.94 ng/mL |
Sample Volume | 50μL |
Sample Type | serum, plasma and other biological fluids |
Specificity | This kit recognizes Universal 5-HIAA in samples.No significant cross-reactivity or interference between Universal 5-HIAA and analogues was observed |
Precision | Both intra-CV and inter-CV are < 10%. |
Recovery | 80%-120% |
Introduction | This ELISA kit applies to the in vitro quantitative determination of 5-HIAA concentrations in serum, plasma and other biological fluids. |
Applications | ELISA |
Storage | 2-8℃/-20℃ |
Test Principle
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Universal 5-HIAA. During the reaction, Universal 5-HIAA in the sample or standard competes with a fixed amount of Universal 5-HIAA on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Universal 5-HIAA. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of Universal 5-HIAA in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Kit Components and Storage
An unopened kit can be stored at 2-8℃ for 1 month. If the kit is not supposed to be used within 1 month, store the items separately according to the following conditions once the kit is received.
Item | Specifications | Storage |
Micro ELISA Plate(Dismountable) | 96T: 8 wells ×12 strips | -20℃, 6 months |
48T: 8 wells ×6 strips | ||
Reference Standard | 96T: 2 vials | |
48T: 1 vial | ||
Concentrated Biotinylated Detection Ab (100×) | 96T: 1 vial, 120 μL | |
48T: 1 vial, 60 μL | ||
Concentrated HRP Conjugate (100×) | 96T: 1 vial, 120 μL | -20℃(Protect from light), 6 months |
48T: 1 vial, 60 μL | ||
Reference Standard & Sample Diluent | 1 vial, 20 mL | 2-8°C, 6 months |
Biotinylated Detection Ab Diluent | 1 vial, 14 mL | |
HRP Conjugate Diluent | 1 vial, 14 mL | |
Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
Substrate Reagent | 1 vial, 10 mL | 2-8℃ (Protect from light) |
Stop Solution | 1 vial, 10 mL | 2-8℃ |
Plate Sealer | 5 pieces | |
Manual | 1 copy | |
Certificate of Analysis | 1 copy |
Technical Data:
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and
high level 5-HIAA were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and
high level 5-HIAA were tested on 3 different plates, 20 replicates in each plate,
respectively.
Intra-assay Precision | Inter-assay Precision | |||||
Sample | 1 | 2 | 3 | 1 | 2 | 3 |
n | 20 | 20 | 20 | 20 | 20 | 20 |
Mean (ng/mL) | 204.2 | 588.5 | 1720.2 | 221.1 | 588.2 | 1852 |
Standard deviation | 10.6 | 29.4 | 61.9 | 13.9 | 24.7 | 59.3 |
CV (%) | 5.19 | 5 | 3.6 | 6.29 | 4.2 | 3.2 |
Recovery
The recovery of 5-HIAA spiked at three different levels in samples throughout the
range of the assay was evaluated in various matrices.
Sample Type | Range (%) | Average Recovery (%) |
---|---|---|
Serum(n=8) | 85-98 | 91 |
EDTA plasma(n=8) | 93-106 | 98 |
Cell culture media(n=8) | 92-106 | 99 |
Target Information
Research Area | Neuroscience, Metabolism |
Assay Procedures
1. Add 50μL standard or sample to the wells, immediately add 50μL Biotinylated Detection Ab working solution to each well. Incubate for 45 min at 37°C |
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2. Aspirate and wash the plate for 3 times |
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3. Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times |
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4. Add 90μL Substrate Reagent. Incubate for 15 min at 37°C |
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5. Add 50μL Stop Solution |
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6. Read the plate at 450nm immediately. Calculation of the results |